1. Home
  2. Labeler Index
  3. Tonymoly Co., Ltd.
  4. NDC Product Code: 59078-121 Tonymoly My Sunny Body And Family Sun Cream

NDC 59078-121 Tonymoly My Sunny Body And Family Sun Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59078-121?
  4. Tonymoly My Sunny Body And Family Sun Cream Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59078-121
Proprietary Name:
Tonymoly My Sunny Body And Family Sun Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tonymoly Co., Ltd.
Labeler Code:
59078
Product Label ID:
29ddedc4-e8fc-4b41-e054-00144ff88e88
Start Marketing Date: [9]
01-14-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59078-121-01

Package Description: 1 TUBE in 1 CARTON / 100 mL in 1 TUBE

Product Details

What is NDC 59078-121?

The NDC code 59078-121 is assigned by the FDA to the product Tonymoly My Sunny Body And Family Sun Cream which is product labeled by Tonymoly Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59078-121-01 1 tube in 1 carton / 100 ml in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Tonymoly My Sunny Body And Family Sun Cream?

Take an appropriate amount, evenly apply to face and body anywhere to be exposed to UV rays. Use as the last step of basic skin care.

Which are Tonymoly My Sunny Body And Family Sun Cream UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Tonymoly My Sunny Body And Family Sun Cream Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".